Title of article :
1,4-Addition of an aryllithium reagent to diethyl ketomalonate. Scalable synthesis of ethyl 1-(hydroxymethyl)-1,3-dihydroisobenzofuran-1-carboxylate
Author/Authors :
Rocke، نويسنده , , Benjamin N. and Conn، نويسنده , , Edward L. and Eisenbeis، نويسنده , , Shane A. and Ruggeri، نويسنده , , Roger B.، نويسنده ,
Issue Information :
هفته نامه با شماره پیاپی سال 2012
Pages :
4
From page :
5467
To page :
5470
Abstract :
While optimizing the synthesis of pharmaceutical building block 3 [ethyl 1-(hydroxymethyl)-1,3-dihydroisobenzofuran-1-carboxylate], we encountered an unusual addition of an aryllithium reagent to the ketone oxygen atom of diethyl ketomalonate. Compound 3 was ultimately prepared on a large scale by a two-step sequence involving (1) annulation of a functionalized Grignard reagent with diethyl ketomalonate and (2) selective mono-reduction of a geminal diester using lithium tri-tert-butoxyaluminum hydride.
Keywords :
Directed ortho metalation , 1 , 4-addition , annulation , Mono-reduction , Diethyl ketomalonate
Journal title :
Tetrahedron Letters
Serial Year :
2012
Journal title :
Tetrahedron Letters
Record number :
1882212
Link To Document :
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